A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561645



Internal ID16002368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:51744386..51831115hg38UCSC Ensembl
Innerchr13:52318522..52405251hg19UCSC Ensembl
Innerchr13:51216523..51303252hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3886730
hg1986730
hg1886730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3146n54
Supporting Variantsnssv811669
Samples
Known GenesDHRS12, LINC00282, WDFY2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer